MOWAT-WILSON SYNDROME: DEEP PHENOTYPING AND MOLECULAR CHARACTERISATION OF TWELVE NEW INDIVIDUALS

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dc.contributor.authorAltunoglu, Umut
dc.contributor.authorGunes, Nilay
dc.contributor.authorTurgut, Gozde Tutku
dc.contributor.authorKalayci, Tugba
dc.contributor.authorAslanger, Ayca Dilruba
dc.contributor.authorDerbent, Murat
dc.contributor.authorEraslan, Serpil
dc.contributor.authorKaraman, Birsen
dc.contributor.authorUyguner, Zehra Oya
dc.contributor.authorTuysuz, Beyhan
dc.contributor.authorAlanay, Yasemin
dc.contributor.authorKayserili, Hulya
dc.date.accessioned2025-10-16T15:12:09Z
dc.date.issued2025
dc.identifier.doi10.26650/IUITFD.1597597
dc.identifier.otherWOS:001399857200001
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/5272
dc.publisherISTANBUL UNIV, FAC MEDICINE, PUBL OFF
dc.sourceJOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI
dc.subjectMowat\\-Wilson syndrome
dc.subjectZEB2
dc.subjectintellectual disabili\\- ty
dc.subjectCHARGE syndrome
dc.subjectAicardi syndrome
dc.titleMOWAT-WILSON SYNDROME: DEEP PHENOTYPING AND MOLECULAR CHARACTERISATION OF TWELVE NEW INDIVIDUALS
dc.typeArticle

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